Bard recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector problems that may prevent catheter insertion or locking. Affected units have specific model and lot numbers.
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
Bard is recalling Grosh:ng NXT ClearVue Catheters with Sherlock Tip Location System because the distal connector may be too narrow or deformed, making it hard to insert or lock the catheter properly. This could lead to failed catheter placements or improper connections.
The distal connector may be too narrow, causing the catheter to get stuck during insertion. It may also be deformed, preventing the catheter from locking securely in place. Both issues could lead to failed catheter placements or improper connections.
Healthcare professionals using the catheter for central venous access are most likely affected. Patients receiving catheter treatments may also be impacted if the device fails to function correctly.
Check for the model number REF CK000379 on the catheter packaging or label. The product includes lot numbers redx1384, reep414: reeq1238. This catheter is designed for central venous catheterization.
Look for the model number REF CK000379 and lot numbers redx1384, reep4143, reeq1238 on the catheter packaging or label.
The distal connector may be too narrow or deformed, causing the catheter to get stuck during insertion or fail to lock securely.
Check the model number and lot numbers on the packaging or label to confirm if it's affected. Bard does not provide a specific remedy for this recall.
The recall record does not mention any remedy or fix for the catheter issues.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1666-2021 — Bard Bard Hello, I own a Bard that is covered by recall Z-1666-2021 from Bard. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
